Research Nurse Coordinator

Actalent • Orlando, FL

375d • $83,200 - $98,000

About The Position

Actively Hiring Clinical Research Nurse Opportunity in Orlando, FL. This position involves delivering safe care and demonstrating regard for the dignity and respect of all participants. The Clinical Research Nurse will maintain skills in clinical competencies including physical assessment, phlebotomy, and IV insertion, while practicing the principles of Universal Precautions and understanding HIPAA regulations. The role requires maintaining a clean, prepared clinical space, performing set-up and turnover procedures in all clinical areas per SOPs, and participating in internal and/or external training programs to maintain licensure. Effective communication with healthcare team members, patients, investigators, sponsors of research, and administration is essential. The nurse will review all elements of the current institutional IRB approved informed consent document with study candidates and/or legal representatives, manage multiple clinical trial protocols, and ensure accurate documentation and management of records, study medication, and test articles confidentially and securely. Additionally, the nurse will promote PI oversight and coordinate the work of support staff, laboratory technicians, and assistants to ensure efficient, timely, and high-quality results and adherence to research protocols.

Requirements

• Must have experience consenting and enrolling participants in clinical trials
• Ability to perform clinical tasks including assisting physicians and CRN with minor procedures and other study requirements within scope of practice.
• Ability to acclimate and integrate into various clinical settings as needed per protocol.
• Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion, and administration of investigational drugs.
• Associate degree in Nursing
• Minimum 2 years of Clinical Research experience
• Current, active State of Florida license as a Registered Nurse
• BLS certification

Responsibilities

• Deliver safe care and demonstrate regard for the dignity and respect of all participants.
• Maintain skills in clinical competencies including physical assessment, phlebotomy, and IV insertion.
• Practice the principles of Universal Precautions and understand HIPAA regulations.
• Maintain a clean, prepared clinical space, and perform set-up and turnover procedures in all clinical areas per SOPs.
• Participate in internal and/or external training programs to maintain licensure.
• Utilize positive interpersonal communication skills; communicate effectively with healthcare team members, patients, investigators, sponsors of research, and administration.
• Review all elements of the current institutional IRB approved informed consent document with study candidates and/or legal representatives.
• Manage multiple clinical trial protocols, coordinate execution and follow-up, utilize resources, and work independently.
• Perform accurate, legible, and timely documentation; manage records, study medication, and test articles confidentially and securely.
• Promote PI oversight by advising the PI, sub-investigators, Supervisor, and/or Clinical Operations Manager of deviations in conduct, patient status, and issues relevant to trial integrity and subject safety.
• Coordinate the work of support staff, laboratory technicians, and assistants to ensure efficient, timely, and high-quality results and adherence to research protocols.

Benefits

• Paid Days Off from Day One
• Career Development
• Whole Person Wellbeing Resources
• Mental Health Resources and Support
• Pet Insurance*
• Debt-free Education* (Certifications and Degrees without out-of-pocket tuition expense)

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Administrative and Support Services
• Education Level: Associate degree
• Number of Employees: 1,001-5,000 employees